TG Chromosome 8

Thyroglobulin
307 variants 307 Health Risk

Upload your DNA to see your personal genotypes for variants in TG.

What This Gene Does
Thyroglobulin (Tg) is a glycoprotein homodimer produced predominantly by the thryroid gland. It acts as a substrate for the synthesis of thyroxine and triiodothyronine as well as the storage of the inactive forms of thyroid hormone and iodine. Thyroglobulin is secreted from the endoplasmic reticulum to its site of iodination, and subsequent thyroxine biosynthesis, in the follicular lumen. Mutations in this gene cause thyroid dyshormonogenesis, manifested as goiter, and are associated with moderate to severe congenital hypothyroidism. Polymorphisms in this gene are associated with susceptibility to autoimmune thyroid diseases (AITD) such as Graves disease and Hashimoto thryoiditis. [provided by RefSeq, Nov 2009]
Associated Conditions (16)
Iodotyrosyl coupling defect
Inborn genetic diseases
TG-related disorder
Autoimmune thyroid disease
susceptibility to
3
Thyroid cancer
nonmedullary
1
Ovarian serous cystadenocarcinoma
Congenital hypothyroidism
Acute myeloid leukemia
Lung cancer
Premature ovarian failure
Gastric cancer
Hypothyroidism
Key Variants
RS1022148195
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
Health Risk
RS111363334
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Inborn genetic diseases, Iodotyrosyl coupling defect
Health Risk
RS112300885
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
Health Risk
RS114211101
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
Health Risk
RS114305064
Conflicting classifications of pathogenicity
Inborn genetic diseases, TG-related disorder, Inborn genetic diseases
Health Risk
RS114322847
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
Health Risk
RS114436500
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, TG-related disorder, Iodotyrosyl coupling defect
Health Risk
RS114477962
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
Health Risk
RS114613744
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
Health Risk
RS114781869
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Autoimmune thyroid disease, susceptibility to
Health Risk
RS114875802
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
Health Risk
RS114944116
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Thyroid cancer, nonmedullary
Health Risk
All Variants (307)
RSID Category Clinical Significance Conditions
RS2491012385 Health Risk Pathogenic
RS2491114233 Health Risk Pathogenic Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
RS2491240602 Health Risk Pathogenic
RS2536862285 Health Risk Pathogenic
RS2536862352 Health Risk Pathogenic Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
RS2536863410 Health Risk Pathogenic
RS2536863682 Health Risk Pathogenic
RS2536873718 Health Risk Pathogenic
RS2537569171 Health Risk Pathogenic
RS2537570064 Health Risk Pathogenic
RS2537716968 Health Risk Pathogenic
RS2537814830 Health Risk Pathogenic
RS2537824316 Health Risk Pathogenic
RS2537825200 Health Risk Pathogenic
RS374620255 Health Risk Pathogenic Congenital hypothyroidism, Iodotyrosyl coupling defect, TG-related disorder
RS375424292 Health Risk Pathogenic Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
RS531772882 Health Risk Pathogenic
RS555316512 Health Risk Pathogenic
RS573918155 Health Risk Pathogenic
RS745902921 Health Risk Pathogenic
RS746023979 Health Risk Pathogenic
RS748309986 Health Risk Pathogenic
RS752966476 Health Risk Pathogenic Iodotyrosyl coupling defect, Autoimmune thyroid disease, susceptibility to
RS754658907 Health Risk Pathogenic Autoimmune thyroid disease, susceptibility to, 3
RS755777744 Health Risk Pathogenic
RS756225459 Health Risk Pathogenic
RS759171140 Health Risk Pathogenic
RS760105184 Health Risk Pathogenic
RS763447736 Health Risk Pathogenic
RS764514762 Health Risk Pathogenic
RS768907494 Health Risk Pathogenic
RS771718064 Health Risk Pathogenic
RS772956775 Health Risk Pathogenic
RS773142559 Health Risk Pathogenic Iodotyrosyl coupling defect, Autoimmune thyroid disease, susceptibility to
RS775044481 Health Risk Pathogenic
RS776553164 Health Risk Pathogenic Autoimmune thyroid disease, susceptibility to, 3
RS777825620 Health Risk Pathogenic
RS778849740 Health Risk Pathogenic Iodotyrosyl coupling defect, TG-related disorder, Iodotyrosyl coupling defect
RS779043995 Health Risk Pathogenic Autoimmune thyroid disease, susceptibility to, 3
RS780765199 Health Risk Pathogenic
RS780846892 Health Risk Pathogenic Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
RS890862536 Health Risk Pathogenic
RS962077113 Health Risk Pathogenic
RS971873834 Health Risk Pathogenic
RS137854434 Health Risk Pathogenic/Likely pathogenic Iodotyrosyl coupling defect, TG-related disorder, Autoimmune thyroid disease
RS142308887 Health Risk Pathogenic/Likely pathogenic Iodotyrosyl coupling defect, Autoimmune thyroid disease, susceptibility to
RS1554648860 Health Risk Pathogenic/Likely pathogenic
RS1554681801 Health Risk Pathogenic/Likely pathogenic
RS16904774 Health Risk Pathogenic/Likely pathogenic Iodotyrosyl coupling defect, Autoimmune thyroid disease, susceptibility to
RS199599591 Health Risk Pathogenic/Likely pathogenic Iodotyrosyl coupling defect, Autoimmune thyroid disease, susceptibility to
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